Technical Writer II (IT)

Title:

Technical Writer II (IT)

Duration:

9 months

Location:

1 Discovery Dr, Swiftwater, PA 18370 (Onsite)

Schedule:

Monday-Friday, 8:00 AM - 4:30 PM (slight flexibility)

Description:

The One LIMS EM project technical writer is responsible for supporting on-time implementation of OneLIMS EM global system for the Swiftwater, PA site. The candidate must perform tasks in an efficient, cGMP compliant, and safe manner. Success in this position requires the individual to be adaptable and react quickly to changing priorities in a high-stress environment. The candidate is required to complete Safety and Compliance training and associated training modules.

key responsibilities:

Design, develop, and update required technical documentation Assist with the editing of quality documents (SOP's, guidelines, validation master plans, etc.) to ensure compliance with regulatory requirements Create Training slides and content Support Future State Process Mapping Organize, track and plan master data review Track and mange project specific deliverables

Qualifications:

Bachelor's Degree required. Prior experience with quality applications, such as Veeva, LIMS Prior experience with MS Word, Excel, Powerpoint, Visio and Outlook Prior work experience in a good manufacturing practices (GMP) environment Must possess sound interpersonal and information gathering skills, be able to relate well to others and have the ability to work in a team environment, effectively interacting with others Excellent verbal and written communication skills. Minimum of 2 + years of related experience. Role will work with a team on a new digital system to convert information into training materials. Free parking available

Required Experience/Skills:

Minimum bachelor's degree required; master's and PhD candidates are welcome Preferred areas of study: IT or sciences Minimum of 2+ years of experience in a similar role; more years of experience is acceptable. Nice-to-Have /

Preferred Skills:

Background in digital IT or scientific fields Experience with QC (quality control) activities Experience with LIMS systems (e.g., LabVantage, iLMS, Sequel, or related systems) Experience deploying digital systems (e.g., LabWare, LIMS) strongly preferred Knowledge of validation processes is a plus Previous experience in pharmaceutical, analytical, or biotech environments (e.g., Veeva) preferred Proficiency in PowerPoint with the ability to create training materials, including slides and graphics Strong presentation skills